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Enhanced apoptosis under low serum conditions in human glioblastoma cells by connexin 43 (Cx43)

  • Ruochun Huang
  • , Ya Guang Liu
  • , Ying Lin
  • , Yan Fan
  • , Alton Boynton
  • , Dongzi Yang
  • , Ruo Pan Huang

Research output: Contribution to journalArticlepeer-review

Abstract

Connexin 43 (Cx43), a structural component of gap junctions, is believed to function as a tumor suppressor gene. Previously, we showed that expression of Cx43 suppresses cell proliferation and tumorigenicity of human glioblastoma cells [Huang et al., Cancer Res 58:5089-5096, 1998] and enhances apoptosis in response to chemotherapeutic agents [Huang et al., Int J Cancer 92:130-138, 2001]. In the present study, we demonstrated that expression of Cx43 in human glioblastoma cells potentiated an apoptotic program under low-serum conditions. The Cx43-mediated effect was coupled with a decreased expression of the specific apoptosis-inhibitor bcl-2. Overexpression of bcl-2 in Cx43-transfected cells conferred resistance to apoptosis induced under low-serum conditions, suggesting that the Cx43-mediated apoptosis under low-serum conditions is regulated, in part, through the downregulation of bcl-2 expression. Furthermore, application of the phosphatidylinositol-3'-OH kinase inhibitor LY294002 specifically induced apoptosis in Cx43-transfected cells. Our results demonstrate a new role of Cx43 in the mediation of apoptosis under low serum conditions.

Original languageEnglish (US)
Pages (from-to)128-138
Number of pages11
JournalMolecular Carcinogenesis
Volume32
Issue number3
DOIs
StatePublished - 2001
Externally publishedYes

Keywords

  • Apoptosis
  • Connexin 43
  • Human glioblastoma
  • Phosphatidylinositol-3′-OH kinase
  • bcl-2

ASJC Scopus subject areas

  • Molecular Biology
  • Cancer Research

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